Epitope Landscape in Breast and Colorectal Cancer

American Association for Cancer Research (AACR) - Tập 68 Số 3 - Trang 889-892 - 2008
Neil H. Segal1,2, D. Williams Parsons3, Karl S. Peggs2,4, Victor E. Velculescu3, Ken W Kinzler3, Bert Vogelstein3, James P. Allison2,4
11Department of Medicine,
22Ludwig Center for Cancer Immunotherapy, and
34Ludwig Center for Cancer Genetics and Therapeutics at The Johns Hopkins Kimmel Cancer Center, Baltimore, Maryland
43Immunology Program, Memorial Sloan-Kettering Cancer Center, New York, New York; and

Tóm tắt

Abstract

The finding that individual cancers contain many mutant genes not present in normal tissues has prompted considerable interest in the cancer epitope landscape. To further understand such effects, we applied in silico–based epitope prediction algorithms and high throughput post hoc analysis to identify candidate tumor antigens. Analysis of 1,152 peptides containing missense mutations previously identified in breast and colorectal cancer revealed that individual cancers accumulate on average ∼10 and ∼7 novel and unique HLA-A*0201 epitopes, respectively, including genes implicated in the neoplastic process. These data suggest that, with appropriate manipulation of the immune system, tumor cell destruction in situ may provide a polyvalent tumor vaccine without a requirement for knowledge of the targeted antigens. [Cancer Res 2008;68(3):889–92]

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